Canonical Allele Identifier: PA2828716004
Gene: BBS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 285261

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364385.1:p.Ser70Asn
CA8066097
NM_001377456.1:c.209G>A